Does KETOTIFEN Cause Product container issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product container issue have been filed in association with KETOTIFEN (Eye Itch Relief). This represents 0.1% of all adverse event reports for KETOTIFEN.
6
Reports of Product container issue with KETOTIFEN
0.1%
of all KETOTIFEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From KETOTIFEN?
Of the 6 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOTIFEN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does KETOTIFEN Cause?
Treatment failure (3,038)
Drug ineffective (798)
Eye irritation (455)
Eye pain (208)
Ocular hyperaemia (166)
Eye pruritus (164)
Hypersensitivity (102)
Vision blurred (87)
Condition aggravated (83)
Eye swelling (72)
What Other Drugs Cause Product container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
Which KETOTIFEN Alternatives Have Lower Product container issue Risk?
KETOTIFEN vs KLONOPIN
KETOTIFEN vs L-ASPARAGINASE
KETOTIFEN vs LABETALOL
KETOTIFEN vs LABETALOL\LABETALOL
KETOTIFEN vs LACIDIPINE